Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Cacna1a and childhood absence epilepsy in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Tokuda S, etal., Brain Res. 2006 Dec 28;.
  • The annotation has been inferred from sequence orthology with Cacna1a (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 12 additional annotations were made from Tokuda S, etal., Brain Res. 2006 Dec 28;.
  • 26 RGD objects have been annotated to childhood absence epilepsy  (DOID:1825)
  • 22 papers in RGD have been used to annotate Cacna1a
  • Curation Notes: DNA:mutation:cds:752T>A (p.M251K)(rat)

  • This annotation was curated on 2018-04-28 09:02:01.0 by RGD . For more information contact us

    An association has been curated linking Cacna1a and childhood absence epilepsy in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with CACNA1A (Homo sapiens) [(EXP) inferred from experiment]
  • 26 RGD objects have been annotated to childhood absence epilepsy  (DOID:1825)
  • 22 papers in RGD have been used to annotate Cacna1a
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17196942

  • This annotation was curated on 2019-10-01 04:43:52.0 by RGD . For more information contact us

    Go Back to source page   Continue to Ontology report



    NHLBI Logo

    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.